Metal oxide nanofibrous materials for photodegradation of environmental toxins

Metal oxide nanofibrous materials for photodegradation of environmental toxins
US10661261

Mixed-phase TiO_{2 #2# nanofibers prepared via a sol-gel technique followed by electrospinning and calcination are provided as photocatalysts. The calcination temperature is adjusted to control the rutile phase fraction in TiO₂nanofibers relative to the anatase phase. Post-calcined TiO₂nanofibers composed of 38 wt % rutile and 62 wt % anatase exhibited the highest initial rate constant of UV photocatalysis. This can be attributed to the combined influences of the fibers' specific surface areas and their phase compositions.}

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Patent 10661261
Priority Mar 13 2015
Filed Mar 14 2016
Issued May 26 2020
Expiry Mar 21 2039 Extension 1102 days
Inventors Liu, Jian
Assg.orig The Resear…
Assg.curr The Resear…
Entity Large
Referenced by 0
References 67
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CROSS REFERENCE TO R…
GOVERNMENT LICENSE R…
FIELD OF THE INVENTI…
BACKGROUND OF THE IN…
SUMMARY OF THE INVEN…
BRIEF DESCRIPTION OF…
DETAILED DESCRIPTION…
Example 1
Example 2
Example 3
Example 4
Example 5

#2# 19. A metal oxide nanofiber, comprising a phase heterogeneous titanium dioxide crystalline material comprising a rutile phase with an x-ray diffraction pattern having a 2 theta value of about 25.5° and an anatase phase with an x-ray diffraction pattern having a 2 theta value of about 27.6° formed by calcination of small molecule titanium oxide sol-gel precursors, adapted for photoexcitation of chemically-reactive electron-hole pairs in proximity to susceptible molecules that results in formation of reactive radical species from both the conduction band and the valence band.

#2# 1. A metal oxide crystalline nanofiber comprising:

titanium dioxide comprising a rutile phase and an anatase phase, calcined from common precursor molecules, the metal oxide crystalline nanofiber having a heterogeneous phase structure material characterized by an x-ray diffraction pattern having 2 theta values of about 25.5° representing the anatase phase and about 27.6° representing the rutile phase,

wherein photoexcitation of chemically-reactive electron-hole pairs in the metal oxide crystalline nanofiber in proximity to susceptible molecules results in formation of reactive radical species from both the conduction band and the valence band.

2. #2# The metal oxide nanofiber according to claim 1, wherein a ratio of the rutile phase to the anatase phase is at least 3:97.

3. #2# The metal oxide nanofiber according to claim 1, formed by a process of electrospinning of nanofibers comprising the precursor molecules, and subsequent calcining.

4. #2# The metal oxide nanofiber according to claim 1, further comprising at least one of a catalytic metal and graphene.

5. #2# The metal oxide nanofiber according to claim 1, further comprising a metal-organic framework (MOF).

6. #2# The metal oxide nanofiber according to claim 1, further comprising a Poly(3,4-ethylenedioxythiophene) (PEDOT) surface film.

7. #2# The metal oxide nanofiber according to claim 1, further comprising a dye which interacts with light to at least one of:

elevate an electron in the titanium dioxide into a conduction band; and

produce a hole by transferring an electron in the titanium dioxide to the valence band.

8. #2# The metal oxide nanofiber according to claim 1, further comprising a dopant in the titanium oxide adapted to induce semiconductivity.

9. #2# The metal oxide nanofiber according to caim 1, wherein:

the rutile phase of the metal oxide nanofiber is adapted to absorb photons, form hydroxyl radicals and hydrogen anions from surface absorbed hydroxyl, and to transfer electrons to the anatase phase of the metal oxide nanofiber; and

the anatase phase of the metal oxide nanofiber is adapted to absorb photons, form superoxide radicals from surface absorbed oxygen, and receive electrons from the rutile phase of the metal oxide nanofiber.

10. #2# The metal oxide nanofiber according to claim 1, produced by a method, comprising:

forming a polymeric suspension of titanium oxide sol-gel precursor;

electrospinning the polymeric suspension to form a fibrous layer; and

calcining the fibrous layer at a controlled temperature, to degrade polymers of the polymeric suspension, to produce the metal oxide nanofiber, wherein the metal oxide nanofiber is photoctalytic and is photoexcitable to produce electron-hole pairs with an ability to form reactive radical species of proximate molecules from both the conduction band and the valence band.

11. #2# The metal oxide nanofiber according to claim 10, wherein the metal oxide nanofiber have a ratio of rutile phase to anatase phase of at least 3:97.

12. #2# The metal oxide nanofiber according to claim 10, wherein the metal oxide nanofiber further comprises at least one of a catalytic metal and graphene.

13. #2# The metal oxide nanofiber according to claim 10, wherein the metal oxide nanofiber further comprises a metal-organic framework (MOF).

14. #2# The metal oxide nanofiber according to claim 10, wherein the metal oxide nanofiber further comprises a Poly(3,4-ethylenedioxythiophene) (PEDOT) surface film.

15. #2# The metal oxide nanofiber according to claim 10, wherein the metal oxide nanofiber comprises comprise a dye which interacts with light to at least one of:

elevate an electron into a conduction band in the metal oxide nanofiber; and

produce a hole in a valence band electron in the metal oxide nanofiber.

16. #2# The metal oxide nanofiber according to claim 10, wherein the metal oxide nanofiber further comprises a dopant in the titanium oxide which induces semiconductivity.

17. #2# The metal oxide nanofiber according to claim 10, wherein the metal oxide nanofiber comprises respective regions having a distinct rutile phase and a distinct anatase phase,

the rutile phase being adapted to absorb photons, form hydroxyl radicals and hydrogen anions from surface absorbed hydroxyl, and to transfer electrons to an anatase phase; and

the anatase phase is adapted to absorb photons, form superoxide radicals from surface absorbed oxygen, and receive electrons from the rutile phase.

18. #2# The metal oxide nanofiber according to claim 10, wherein the fibrous layer is calcined from the common precursor molecules under conditions that result in a crystalline substantially inorganic solid comprising the anatase phase and the rutile phase.

20. #2# The metal oxide nanofiber according to claim 19, comprising at least 3% rutile phase.

21. #2# The metal oxide nanofiber according to claim 19, wherein the metal oxide nanofiber is photoexcited to form electron-hole pairs, further comprising surface adsorbed molecules and free radicals formed from the surface adsorbed molecules from both the conduction band and the valence band of the photoexcited metal oxide nanofiber.

22. #2# The metal oxide nanofiber according to claim 21, wherein the free radicals comprise hydroxyl radicals and superoxide radicals, the free radicals formed being adapted to degrade an organic compound in a solution surrounding the metal oxide nanofiber.

23. #2# The metal oxide nanofiber according to claim 19, further comprising at least one of a catalytic metal, graphene, a metal-organic framework (MOF), a Poly(3,4-ethylenedioxythiophene) (PEDOT) surface film, and a dopant in the titanium oxide which induces semiconductivity.

24. #2# The metal oxide nanofiber according to claim 19, further comprising a dye which interacts with light to transfer an electron into a conduction band in the titanium dioxide.

25. #2# The metal oxide nanofiber according to claim 19, further comprising a dye which interacts with light to at least one of:

facilitate production of a hole in a valence band electron in the titanium dioxide,

facilitate elevation of an electron to a conduction band in the titanium dioxide.

26. #2# The metal oxide nanofiber according to claim 19, wherein:

CROSS REFERENCE TO RELATED APPLICATIONS

This invention is a non-provisional of U.S. Provisional Patent Application No. 62/132,611, filed Mar. 13, 2015.

GOVERNMENT LICENSE RIGHTS

This invention was made with government support under contract W911NF1310235 awarded by the US Army Research Office. The government has certain rights in the invention.

FIELD OF THE INVENTION

The present invention relates to the field of photocatalytic materials, and more particularly to photocatalytic systems and methods for degrading environmental toxins.

BACKGROUND OF THE INVENTION

The present invention describes subject matter that relates to nanotechnology systems and methods that provide rapid decontamination and protection.

Metal oxide photocatalysts have been regarded as one of the most active areas in heterogeneous catalysis due to their great catalytic abilities for removing environmental pollutants relating to waste water, polluted air, and chemical warfare agents. Compared with other photocatalytic materials, one-dimensional metal oxide nanofibrous materials are particularly attractive due to their high specific surface area, ease of fabrication and functionalization, and versatility in controlling the fiber diameters and morphologies.

The prior art has taught techniques for decontamination of toxic industrial chemicals and chemical warfare agents on building materials using chlorine dioxide fumigant and liquid oxidant technologies.

Many pharmaceutical and medical facility waste streams are considered hazardous and toxic. Hospitals, nursing homes, private clinics, and laboratories are a growing source of this type of environmental pollution [1-3]. Residual and waste drugs are discarded into environmental waters through sewers with human waste or direct disposal causing serious contamination. A number of conventional techniques, such as dilution and incineration [4], are widely used to minimize the impact, however they still cannot be removed from contaminated water efficiently. Advances in the field of chemistry have resulted in many improved methods for environmental cleanup. One main focus of study has been using photocatalysts to degrade environmental pollutants [5-9].

In 1972, Akira Fujishima and Kenichi Honda first reported that titanium dioxide had a photocatalytic activity [10]. Since the initial discovery, TiO₂has become regarded as an efficient photocatalyst for degradation of organic pollutants from water due to its strong oxidative power, high stability, low cost and environmental friendliness [11-18]. The three polymorphs of TiO₂, anatase, rutile and brookite, show very different photocatalytic activities. The photocatalytic activity of TiO₂is related to several different factors including degree of crystallinity, specific surface area, porosity, and crystal size [19-23]. The anatase phase of TiO₂exhibits maximum photocatalytic activity due to its higher adsorption affinity for organic molecules [21] and lower electron-hole recombination rate [25-28].

The most commonly used commercial TiO₂photocatalyst is a nanopowder, which consists of ˜25 wt % rutile and 75 wt % anatase. This Degussa P25, shows improved photocatalytic activity over pure anatase or rutile nanopowder. The synergistic effect between the three different TiO₂phases has been widely reported. Zachariah et al. [22] demonstrated that the photocatalytic activity of mixed-phase TiO₂nanoparticles was a function of rutile content with the maximum photocatalytic activity observed for 40 wt % rutile. Su et al. [29] also investigated the influence of the anatase-to-rutile ratios on their photoreactivities. A TiO₂film with ˜60 wt % anatase and ˜40 wt % rutile exhibited optimal performance and a 50% improved activity compared with pure anatase. However, Pal et al. [30] observed that TiO₂microspheres prepared by spray drying and calcined at 400° C. with 52.2 wt % of rutile phase achieved the best photocatalytic efficiency for degradation of dyes. Boppella et al. [31] found that mixed-phase TiO₂nanoparticles composing 83 wt % brookite and 17 wt % rutile exhibited superior photoactivity compared to Degussa P25 and phase-pure anatase nanocrystals. It is clear that the TiO₂phase compositions and the ratios are the key factors in optimizing photodegradation.

Compared with TiO₂nanoparticles, one dimensional TiO₂nanofibers have attracted considerable attention in recent years for energy applications [32, 33] due to their higher surface-to-volume ratio [34], faster electron diffusion to the surface [35, 36] and improved light absorption through the light scattering within the porous structure [34].

See, U.S. Pat. Nos. 8,956,910; 8,940,244; 8,932,346; 8,921,473; 8,920,491; 8,906,814; 8,900,610; 8,900,292; 8,884,507; 8,864,341; 8,840,863; 8,827,192; 8,815,275; 8,815,273; 8,771,343; 8,721,923; 8,715,855; 8,685,424; 8,684,189; 8,652,229; 8,613,363; 8,585,753; 8,574,615; 8,562,895; 8,540,826; 8,460,790; 8,460,547; 8,449,603; 8,431,149; 8,415,267; 8,414,806; 8,383,539; 8,353,949; 8,329,091; 8,318,126; 8,287,937; 8,263,029; 8,231,980; 8,225,641; 8,221,822; 8,216,961; 8,216,632; 8,197,890; 8,187,620; 8,080,335; 8,071,156; 8,070,797; 8,067,054; 8,066,763; 8,029,554; 8,002,823; 7,981,150; 7,976,915; 7,942,926; 7,938,855; 7,931,683; 7,789,930; 7,718,112; 7,709,597; 7,709,088; 7,655,112; 7,635,518; 7,575,707; each of which is expressly incorporated herein by reference in its entirety.

References (each of which is expressly incorporated herein by reference in their entirety):

[1] Fayez, Abdulla, Hani Abu Qdais, Atallah Rabi, “Site investigation on medical waste management practices in northern Jordan”, Waste Management, 2008, 28, 450-458.
[2] Nemade, Rahul, A R Gajbhiiye, “Need of enhanced biomedical waste management”, International Journal of Research in Engineering and Applied Sciences (IJREAS), 2014, 2, 15-18.
[3] Orias, Frederic, Perrodin, Yves, “Pharmaceuticals in hospital wastewater: Their ecotoxicity and contribution to the environmental hazard of the effluent”, Chemosphere, 2014, 115, 31-39.
[4] Hilal, Hikmat S., Ghazi Y. M. Al-Nour, Ahed Zyoud, Muath H. Helal and Iyad Saadeddin, Solid State Sciences, 2010, 12, 578-586.
[5] Perez-Estrada, L. A., M. I. Maldonado, W. Gernjak, A. Aguera, A. R. Fernandez-Alba, M. M. Ballesteros, S. Malato, “Decomposition of diclofenac by solar driven photocatalysis at pilot plant scale”, Catal. Today, 2005, 101, 219-26.
[6] Boreen, A. L., W. A. Arnold, K. McNeill, “Photodegradation of pharmaceuticals in the aquatic environment: a review”. Aquat. Sci. 2003, 65, 320-41.
[7] Chatzitakis, A., C. Berberidou, I. Paspaltsis, G. Kyriakou, T. Sklaviadis, I. Poulios, “Photocatalytic degradation and drug activity reduction of Chloramphenicol”, Water Res. 2008, 42, 386-394.
[8] Kaniou, S., K. Pitarakis, I. Barlagianni, I. Poulios, “Photocatalytic oxidation of sulfamethazine”, Chemosphere, 2005, 60, 372-80.
[9] Ledakowics, S., M. Soleca, R. Zylla, “Biodegradation, de-colorization and detoxification of textile waste water enhanced by advanced oxidation processes”, J. Biotechnol. 2001, 89, 175-84.
[10] Fujishima, Akira, Honda Kenichi, “Electrochemical Photolysis of Water at a Semiconductor Electrode”, Nature, 238, 5358, 37-8.
[11] Dai, K., H. Chen, T. Peng, D. Ke, H. Yi, “Photocatalytic degradation of methyl orange in aqueous suspension of mesoporous titania nanoparticles”, Chemosphere 69, 2007, 1144-55.
[12] Herrmann, J. M., C. Duchamp, M. Karkmaz, B. T. Hoai, H. Lachheb, E. Puzenat, C. Guillard, “Environmental green chemistry as defined by photocatalysis”, J. of Hazard Mater. 145, 2007, 624-9.
[13] Carp, O., C. L. Huisman, A. Reller, “Photoinduced reactivity of titanium dioxide”, Prog. Solid State Chem. 32, 2004, 33-177.
[14] Bizani, E., K. Fytianos, I. Poulios, V. Tsiridis, “Photocatalytic decolorization and degradation of dye solution and wastewaters in the presence of titanium dioxide”, J. Hazard. Mater. 2006, 136, 85-94.
[15] Hilal, H. S., L. Z. Majjad, N. Zaatar, A. El-Hamouz, “Dye-effect in TiO₂catalyzed contaminant photo-degradation: sensitization vs. charge-transfer formalism”, Solid State Sci. 2007, 9, 9-15.
[16] Dai, K., H. Chen, T. Peng, D. Ke, K. Yi, “Photo catalytic degradation of methyl orange in aqueous suspension of meso porous titania nanoparticles”, Chemosphere, 2007, 69, 1361-67.
[17] Chen, C., Z. Wang, S. Ruan, B. Zou, M. Zhao, F. Wu, “Photo catalytic degradation of C. 1. Acid orange 52 in the presence of Zn-doped TiO₂prepared by a stearic acid gel method”, Dyes Pigm. 2008, 77, 204-209.
[18] Li, Y., X. Li, J. Li, J. Yin, “Photo catalytic degradation of methyl orange by TiO₂-coated activated carbon and kinetic study”, Water Res. 2006, 40, 1119-26.
[19] Tayade, R. J.; Surolia, P. K.; Kulkarni, R. G.; Jasra, R. V. “Photocatalytic Degradation of Dyes and Organic Contaminants in Water Using Nanocrystalline Anatase and Rutile TiO2”, Sci. Technol. Adv. Mater. 2007, 8, 455.
[20] Baiju, K. V.; Shukla, S.; Sandhya, K. S.; James, J.; Warrier, K. G. K. J. Phys. Chem. C 2007, 111, 7612.
[21] Zhang, Z.; Wang, C. C.; Zakaria, R.; Ying, J. Y. J. Phys. Chem. B 1998, 102, 10871.
[22] Zachariah, A.; Baiju, K. V.; Shukla, S.; Deepa, K. S.; James, J.; Warrier, K. G. K. J. Phys. Chem. C 2008, 112, 11345-11356.
[23] Ding, Z.; Lu, G. Q.; Greenfield, P. F. J. Phys. Chem. B 2000, 104, 4815-4820.
[24] Stafford, U.; Gray, K. A.; Kamat, P. V.; Varma, A. Chem. Phys. Lett. 1993, 205, 55-61.
[25] Hurum, D. C.; Agrios, A. G.; Gray, K. A.; Rajh, T.; Thurnauer, M. C. J. Phys. Chem. B 2003, 107, 4545-4549.
[26] Riegel G., and J. R. Bolton, “Photocatalytic Efficiency Variability in TiO2 Particles”, J. Phys. Chem. 1995, 99, 12, 4215-24.
[27] Nagaveni, K.; Sivalingam, G.; Hedge, M. S.; Madras, G. Appl. Catal. B Environ. 2004, 48, 83-93.
[28] Kolar, M.; Mest Ankova, H.; Jirkovsky, J.; Heyrovsky, M.; Subrt, J. Langmuir 2006, 22, 598-604.
[29] Su, Ren, Ralf Bechstein, Lasse So, Ronnie T. Vang, Michael Sillassen, Bjorn Esbjornsson, Anders Palmqvist, and Flemming Besenbacher, J. Phys. Chem. C 2011, 115, 24287-92.
[30] Pal, Sudipto, Anna Maria Laera, Antonio Licciulli, Massimo Catalano, and Antonietta Taurino, I&EC Research, 2014, 53, 7931-38.
[31] Boppella, Ramireddy, Pratyay Basak, and Sunkara V. Manorama, Appl. Mater. & Interfaces, 2012, 4, 1239-46.
[32] Obuya, E. A., W. Harrigan, D. M. Andala, J. Lippens, T. C. Keane, W. E. Jones Jr, Journal of Molecular Catalysis A: Chemical 340 (2011) 89-98.
[33] Obuya, Emilly A., Prakash C. Joshi, Thomas A. Gray, Thomas C. Keane, Wayne E. Jones, Jr. International Journal of Chemistry, 2014, 6, 1-16.
[34] Mingxing Lu, Changlu Shao, Kexin Wang, Na Lu, Xin Zhang, Peng Zhang, Mingyi Zhang, Xinghua Li, and Yichun Liu, Appl. Mater. & Interfaces, 2014, 6, 9004-9012.
[35] Xiang Zhang, Velmurugan Thavasi, S. G. Mhaisalkar and Seeram Ramakrishna, Nanoscale, 2014, 4, 1707-16.
[36] Young-In Lee, Jong-Sik Lee, Eun-Sil Park, Dae-Hwan Jang, Jae-Eun Lee, Kahee Kim, Nosang V. Myung, and Yong-Ho Choa, 2014, 14, 8005-9.
[37] itak, M., S. Ylmaz, Y. Dilgin, G. Türker, S. Yagmur, H. Erdugan, N. Erdugan, Osteryoung “Square wave voltammetric determination of phenazopyridine hydrochloride in human urine and tablet dosage forms based on electrochemical reduction at carbon paste electrode”, Current Pharmaceutical Analysis, 2007, 3, 141-145.
[38] Yagmur, S., S. Yilmaz, M. Sadikoglu, G. Saglikoglu, M. Yildiz, C. Yengin and E. Kilinc, “Electrooxidation of phenazopyridine hydrochloride and its voltammetric and HPLC determination in human urine and tablet dosage form”, Int. J. Electrochem. Sci., 2013, 8, 6818-6828.
[39] David O. Scanlon, Charles W. Dunnill, John Buckeridge, Stephen A. Shevlin, Andrew J. Logsdail, Scott M. Woodley, et al, Nature Materials, 2013, 12, 798-801.
[40] Gibson, H.; Truong, Q.; Walker, J.; Owens, J.; Wander, J.; Jones Jr., W. E. “Chemical and Biological Protection and detection in Fabrics for Protective Clothing”, MRS Bull. 2003, 28(8), 574-578.
[41] Fan, L. J.; Jones Jr., W. E. “A Highly Selective and Sensitive Inorganic/Organic Hybrid Polymer Fluorescence “Turn-on” Chemosensory System for Iron Cations”, J. Am. Chem. Soc., 2006, 128(21), 6784-5.
[42] Fegley, M. E. A.; Pinnock, S. S.; Malele, C. N.; Jones Jr., W. E. “Metal-containing conjugated polymers as fluorescent chemosensors in the detection of toxicants”, Inorg. Chem. Acta. 2012, 381, 78-84.
[43] Rogers, C. W.; Zhang, Y.; Patrick, B. O.; Jones Jr., W. E.; Wolf, M. O. “Photophysical Effect of the Coordination of Water by Ruthenium(II) Bipyridyl Complexes Containing Hemilabile Phosphine-Ether Ligands”, Inorg. Chem. 2002, 41, 1162-1169.
[44] Stengl, V.; Maoikova, M; Bakardjieva, S.; Subrt, J.; Oplustil, F.; Olsanska, M., “Reaction of sulfur mustard gas, soman and VX agent with nanosized anatase TiO2 and ferrihydrite,” J. Chem. Technolo. Biotechnol. 2005, 18, 754-758.
[45] Uddin, M. J.; Cesano, F.; Scarano, D.; Bonino, F.; Agostini, G.; Spoto, G.; Bordiga, S.; Zecchina, A., “Cotton textile fibres coated by Au/TiO2 films: Synthesis, characterization and self cleaning properties”, J. Photochem. Photobiol., A: Chem. 2008, 199 (1), 64-72.
[46] Zhao, X.; Zhao, Q.; Yu, J.; Liu, B., “Development of multifunctional photoactive self-cleaning glasses”, J. Non-Cryst. Solids, 2008, 354, (12-13), 1424-1430.
[47] Madaeni, S. S.; Ghaemi, N., “Characterization of self-cleaning RO membranes coated with TiO2 particles under UV irradiation”, J. Membr. Sci. 2007, 303, 221-233.
[48] Meilert, K.; Laub, D.; Kiwi, J., “Photocatalytic self-cleaning of modified textiles by TiO2 clusters attached by chemical spacers”, J. Mol. Catal., A: Chem. 2005, 237, 101-108.
[49] Textor, T.; Schroter, F.; Schollmeyer, E., “Thin Coatings with Photo-Catalytic Activity Based on Inorganic-Organic Hybrid Polymers Modified with Anatase Nanoparticles”, Macromol. Symp. 2007, 254, 196-202.
[50] Obuya, E.; Harrigan, W.; Andala, D.; Lippens, J.; Keane, T., Jones Jr. W., “Photodeposited Pd Nanoparticle Catalysts Supported on Photoactivated TiO2 Nanofibers” Journal of Mol. Catal., A: Chem., 340, 2011, 89-98.
[51] Obuya, E.; Harrigan, W.; O'Brien, T.; Andala, D.; Mushibe, E.; Jones Jr. W., “Fabrication of Rh-doped TiO2 nanofibers for Visible Light Degradation of Rhodamine B” Mat. Res. Soc. Proc., 2011, 1352.
[52] Liu, Zhaoyang, et al., “An efficient bicomponent TiO2/SnO2 nanofiber photocatalyst fabricated by electrospinning with a side-by-side dual spinneret method,” Nano letters 7.4 (2007): 1081-1085.
[53] Zhan, Sihui, et al., “Long TiO2 hollow fibers with mesoporous walls: sol-gel combined electrospun fabrication and photocatalyti c properties”, The Journal of Physical Chemistry B 110.23 (2006): 11199-11204.
[54] Liu, Ruilai, et al., “Fabrication of TiO2/ZnO composite nanofibers by electrospinning and their photocatalytic property”, Materials Chemistry and Physics 121.3 (2010): 432-439.
[55] Choi, Sung Kyu, et al., “Photocatalytic comparison of TiO₂nanoparticles and electrospun TiO2 nanofibers: effects of mesoporosity and interparticle charge transfer”, The Journal of Physical Chemistry C 114.39 (2010): 16475-16480.
[56] Lee, Sung-Hwan, “Photocatalytic nanocomposites based on TiO₂and carbon nanotubes”. Diss. University of Florida, 2004.
[57] Duchoslav, J., et al., “Electrospun TiO2 Fibers as a Material for Dye Sensitized Solar Cells”, Proc. of NSTI Nanotech Conference, Boston, Mass. 2008.
[58] Wu. Ning, et al., “Preparation and characterization of Fe3+, La3+ Co-doped TiO₂nanofibers and its photocatalytic activity”, J Eng Fibers Fabrics 7 (2012): 16-20,
[59] Sundaramurthy, Jayaraman, et al., “Perspective of electrospun nanofibers in energy and environment”, Biofuel Research Journal 1.2 (2014): 44-54.
[60] Nakane, Koji, and Nobuo Ogata, “Photocatalyst Nanofibers Obtained by Calcination of Organic-Inorganic Hybrids”, INTECH Open Access Publisher, 2010.
[61] Lia, Yue, et al., “High Photocatalytic Activity of CdS modified TiO₂Nanofiber Heteroarchitectures via an Electrospinning Method.”
[62] Memarian, F., and M. Latifi, “Photocatalytic Activity Of TiO₂Nanofibers Fabricated From Polyvinyl Acetate (PVAC).”
[63] Wu, Ning, et al., “Characterization of PVAc/TiO2 hybrid nanofibers: from fibrous morphologies to molecular structures”, Journal of Applied Polymer Science 112.3 (2009): 1481-1485.
[64] Lee, J. S., et al., “Photocatalytic Activity via Synthesis of TiO₂Nanowires Controlled Microstructure and Surface Area by Electrospinning Method.”
[65] Ji, Byung Chul, et al., “Photocatalytic Activity of Electrospun PAN/TiO₂Nanofibers in Dye Photodecomposition.”
[66] Memarian, Farnaz, and Masoud Latifi, “Innovative Fabrication of TiO₂Nanofiber Yarns and Considering Their Photocatalytic Activity.”
[67] Almeida, Nuno, “High efficient TiO2/Eu/graphene visible-light-responsive photocatalysts prepared by electrospinning.”
[68] Ding, Rui, et al., “High sensitive sensor fabricated by reduced graphene oxide/polyvinylbutyral nanofibers for detecting Cu (II) in water.”
[69] Thirugnanam, Lavanya, et al., “A simple and facile route to synthesize anatase/rutile mixed phase TiO₂nanofibers with superior photocatalytic performance”, International Journal of ChemTech Research 6.3 (2014).

SUMMARY OF THE INVENTION

The present technology relates to the application of photocatalysis and an electrospinning process to achieve enhanced photodegradation and decontamination of environmental toxins, such as toxic industrial chemicals (TICs), toxic organic dyes, bio-pharmaceuticals, and chemical warfare agents (CWAs). The present invention and materials have the potential to be utilized in environmental decontamination from chemical and biological contaminants, tissue engineering, drug delivery and clothing/textile self-cleaning applications.

The present technology comprises a composition of one-dimensional nanomaterial electrospun nanofibers. The invention employs the application of photocatalysis and irradiation in the UV or visible region of the spectrum to excite an electron from the valence band (leaving behind a hole) to the conduction band of a semiconductor. These photoinduced charge carriers then proceed to form reactive radicals, e.g., hydroxyl radicals, super oxide, carboxylic acid anion radical, benzyl radical, benzonitrile radical, chalcogenide radical, nitrous oxide radical, sulfoxide radical, etc. that attacks proximate chemicals. Electromagnetic radiation in the form of visible light, ultra-violet light, or even sunlight can be used to achieve enhanced photodegradation that are both rapid and inexpensive compared to the current decomposition techniques that are costly and time consuming. Compared with other photocatalytic materials, one-dimensional nanomaterial electrospun nanofibers have attracted considerable attention due to their high specific surface area to volume ratio, ease of fabrication and functionalization, and versatility in controlling the fiber diameter, morphology, and reactivity. Electrospun nanofibers from stable polymers are ideal candidates for catalytic supports as they can provide a large surface area and a high porosity for catalytic applications. Due to the high surface area to volume ratio, electrospun nanofibers can provide many active anchor sites for doping and bonding with other materials such as graphene and metal-organic frameworks (MOFs).

Nanotechnology can provide novel systems for rapid decontamination and protection through a self-cleaning mechanism. The basic principle of this self-cleaning system is the application of photocatalysis. Nanofibrous photocatalysts use incident irradiation in the UV or visible region of the spectrum to excite an electron from the valence band (leaving behind a hole) to the conduction band of a semiconductor. These photoinduced charge carriers then proceed to form reactive radicals, hydroxyl radicals and super oxide radicals that attack adsorbed chemicals on the surface of the material. Electromagnetic radiation in the form of visible light, ultra-violet light, or even sunlight can be used to achieve enhanced photodegradation that are both rapid and inexpensive compared to the current decomposition techniques that are costly and time consuming. Metal oxide nanofibrous materials represent an alternative approach to conventional composites used in photocatalytic degradation. Their one dimensional morphology is desired compared to traditional nanoparticles; owing to excellent mobility of charge carriers, high surface area to volume ratio, the existence of pores enhancing charge collection and transport. One-dimensional metal oxide nanofibrous materials have attracted considerable attention due to their high specific surface area, ease of fabrication and functionalization, and versatility in controlling the fiber diameter and morphology.

Electrospun nanofibers from stable polymers are ideal candidates for catalytic supports as they can provide a large surface area and a high porosity for catalytic applications. In order to develop novel self-cleaning surfaces and substrates for photodegradation of environmental toxins, some fundamental studies have been investigated on the electrospinning technique, calcination temperature influence on TiO₂phase changes and phase transformation rates of pre-calcined polymer fibers with different diameters. Prepared are a variety of electrospun nanofibrous materials such as, anatase TiO₂, rutile TiO₂, reduced graphene oxide TiO₂, BaTiO₃, platinum nanoparticles supported on anatase TiO₂, ZnO, photoactive dye supported anatase TiO₂. These fibers have been characterized by X-Ray diffraction, Scanning Electron Microscopy, Transmittance Electron Microscopy, Raman Microscopy and Energy-Dispersive X-Ray Spectroscopy. Also, electrospun TiO₂nanofibers show excellent UV degradation results on rhodamine B (Rh.B.), phenazopyridine (PAP) and dimethyl methylphosphonate (DMMP). The photocatalytic activity of pure TiO₂fibers is limited by fast electron-hole pairs' recombination and a relative high energy band gap. Some multifunctional TiO₂fibers have been also fabricated to solve these problems. These novel multifunctional materials offer excellent mobility of charge carriers for faster degradation and the possibility to exploit catalytic processes in decontamination.

The preferred fabrication process takes advantage of an electrospinning process, a non-mechanical, electrostatic process that can produce fibers in the nanometer to micrometer range using electrically driven jets of polymer solution or melts. In this process, a high electric field is created between the polymer fluid and an electrically conducting collector screen. At a critical electrical potential which overcomes surface viscosity, a thin jet is produced from the charged polymer fluid at the tip of a pipette or syringe needle. The solvent evaporates rapidly as the jet is drawn through the air to the collector screen where dry fibers accumulate to produce a mat of nanofibers. The obtained polymer fibers are often allowed time to undergo hydrolysis and polycondensation reactions, followed by thermal treatment in order to favor structural stability via sintering, densification, grain growth and phase transformation. Some fundamental studies have been investigated on the electrospinning technique, calcination temperature influence on TiO₂phase changes and phase transformation rates of pre-calcined polymer fibers with different diameters. Some multifunctional TiO₂nanofibers have been also fabricated to improve the photodegradation performance in visible light irradiation. This technology can be used for treatment of polluted waste water, for the improvement of gas masks, for integration with conventional textiles for self-decontaminating garments, and for spray treatments of combat vehicles.

For synthesis procedure, sol-gel method may be used to get the pre-electrospinning solution. A 1:2 weight ratio of polymethylmethacrylate (PMMA):titanium isopropoxide (TIP) was prepared by completely dissolving PMMA in chloroform followed by drop wise addition of TIP with continuous stirring of the reaction mixture for complete dissolution. Small amount of dimethylformamide (DMF) was added to increase the dielectric constant of the composite solution and hence enable the electrospinning process at a high voltage. For example the range of ratios between preformed polymer and nanoparticle precursor is about 1:1 to 1:10. The hydrophobic nature of both PMMA and TIP enabled the formation of a homogeneous solution of the polymer blend. Electrospinning is a non-mechanical, electrostatic process that produces fibers in the nanometer to micrometer range using electrically driven jets of polymer solution. 15-40 kV (˜1 kV/cm, acceptable range 0.5 kV/cm to 5 kV/cm) was applied across the syringe needle and the collector screen where the PMMA/TIP solution was spun into composite nanofibers and deposited as a randomly oriented non-woven mat on the collector screen. These polymer fibers were left overnight to undergo hydrolysis reactions, followed by thermal treatment in order to favor structural stability via sintering, densification, grain growth and phase transformation.

During the calcination process, the calcination temperatures are high enough to form TiO₂nanofibers, but are low enough to keep the metal-organic frameworks (MOFs) from degradation. The calcination temperatures typically range from 275° C.-325° C., with a target temperature of 300° C. Based on these calcination temperatures, TiO₂nanofibers show different phase combination, pure anatase, pure rutile or their mixture. The X-ray diffraction (XRD) shows that pure anatase phase of TiO₂shows up at relative lower temperature and it begins to transfer to rutile phase as the temperature increases. It is shown under the same calcination condition polymer fibers with larger diameters have a faster anatase to rutile transformation rates and larger grain sizes.

PMMA/TIP polymer fibers with different diameters can be fabricated by altering the parameters used in sol-gel preparation and electrospinning process.

Novel multifunctional TiO₂fibers include the incorporation of UV, Visible and near IR dyes, such as the N3 dye, to form dye sensitized TiO₂nanofibers for photodegradation of PAP under visible light. N3-dye, for example, can absorb visible light and can get excited to generate free electrons to transfer TiO₂, which enlarge the application of TiO₂-based photocatalyst. Alternate dyes may include e.g., coumarins, poryphyrins, anthracene, other metal-to-ligand charge transfer dyes (MLCT), thphalacyanines, perylenes.

It is therefore an object to provide a metal oxide nanofiber comprising a crystalline material comprising titanium dioxide having a relative ratio of rutile to anatase of at least 3:97, calcined from small molecule precursors, wherein photoexcitation of electron-hole pairs results in an ability to form reactive radical species of proximate molecules from both the conduction band and the valence band.

It is also an object to provide a method of forming a photocatalyst fiber, comprising: forming a polymeric syspension of titanium oxide precursor; electrospinning the polyol suspension to form a fibrous layer; and calcining the fibrous layer, to produce photocatalytic titanium oxide fibers having a ratio of rutile to anatase of at least 3:97, wherein the photocatalyst fiber is photoexcitable to produce electron-hole pairs with an ability to form reactive radical species of proximate molecules from both the conduction band and the valence band.

It is a still further object to provide a photocatalytic method, comprising: providing nanofibers calcined from small molecule titanium oxide precursors to form a crystalline material comprising titanium dioxide having a relative ratio of rutile to anatase of at least 3:97; photoexciting the nanofibers to form electron-hole pairs; and forming free radicals from surface adsorbed molecules from both the conduction band and the valence band of the photoexcited nanofibers.

The nanofibers may be formed by a process of electrospinning.

The nanofibers may further comprise a catalytic metal, graphene, a dopand, such as to induce semiconductivity in the titanium dioxide, a metal-organic framework (MOF), a UV, visible or infrared dye, especially a chemically reactive dye which either is photoexcitable to transfer an electron to the conduction band of the titanium dioxide, or to transfer a hole (receive an electron) from the valence band of the titanium dioxide.

The nanofibers may comprise a rutile phase and an anatase phase, wherein the rutile phase is adapted to absorb photons, form hydroxyl radicals and hydrogen anions from surface absorbed hydroxyl, and to transfer electrons to the anatase phase; and the anatase phase is adapted to absorb photons, form superoxide radicals from surface absorbed oxygen, and receive electrons from the rutile phase.

The nanofibers may be formed from a polymeric syspension of titanium oxide precursor.

The nanofibers are preferably calcined under such conditions that result in a crystalline substantially inorganic solid having a predetermined ratio of anatase to rutile. For example, the rutile to anatase ratio may be about 38:72. It is particularly noted that, by providing mixed species of titanium dioxide crystalline domains, the separate effects of conduction band excitation and reaction with oxygen to form superoxide, and valence band interaction of water or hydroxyl to form hydroxyl radical or carboxy radical, with electron transfer between the two domains, the photocatalytic activity may be optimized, and generally increased, over a pure anatase or pure rutile nanofiber. The ratio of crystalling forms is controlled by the calcination conditions, such as temperature, humidity, etc.

The nanofibers may be used for breakdown or modification of various chemicals and pollutants. One embodiment provides a gasmask employing a filter comprising the nanofibrous sheet, which is moistened and illuminated with ultraviolet light during use. Volatile organic compounds in the air interact with free radicals generated from oxygen and moisture adsorbed to the nanofibers, which are then broken down. Similarly, a photocatalytic air filter for an HVAC system can also be provided. The nanofibers may also be used within a water processing system to treat/disinfect water, such as tapwater, to degrade pollutants and kill microorganisms. The nanofibers may also used in a system to activate a stream of water, such as for clothes and dishwashing machines, to reduce reliance on chlorine bleach and reduce detergent consumption. The nanofibers may also be used as photoinitiators in processes that require free radical species. Further, the nanofibers may be used in medical applications to provide targeted toxic therapies, such as skin lesions, neoplasia and tumors, and the like, as well as in certain cosmetic procedures. The UV light may come from sunlight, fluorescent/gas discharge lamps, ultraviolet light emitting diodes, or other known sources. In doped or dye linked embodiments, the photoexcitation may be visible or infrared illumination, and for example this is advantageous in medical and cosmetic environments where the ultraviolet illumination is to be avoided. On the other hand, in broadband illumination such as sunlight, one or more photoexcitable dyes may be used to increase efficiency of use of available energy.

The nanofibers may be used in a process to treat an effluent stream, such as an aqueous environmental runoff or industrial waste steam, having a degradable contaminant molecule (e.g., an organic molecule). Illumination of the nanofibers, such as with sunlight, results in generation of hydroxyl radicals and superoxide radicals from water, which degrade the contaminant(s).

These and other objects will become apparent.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other features and advantages of the present invention will become more readily appreciated as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:

FIG. 1 shows a schematic figure showing three typical processes of fabricating TiO₂nanofibers including sol-gel method, electrospinning technique and calcination treatment.

FIG. 2 shows scanning Electron Microscopy images of (a) pre-calcined polymer nanofibers; post-calcined TiO₂nanofibers at (b) 285° C., (c) 320° C., (d) 360° C., (e) 400° C., (f) 600° C. for 4 hours under ambient atmosphere.

FIG. 3 shows X-ray diffraction patterns of post-calcined TiO₂nanofibers after 285° C., 320° C., 360° C., 400° C. & 600° C. calcinations for 4 hours under ambient atmosphere, where the “A” and “R” in the figure denote the anatase and rutile phases of TiO₂, respectively.

FIG. 4 shows PAP concentration changes based on liquid UV-Vis spectroscopy on aliquots picked up at T=−60, −30, 0, 10, 20, 30, 45, 60 using TiO₂nanofibers with different rutile fractions.

FIG. 5 shows first 30-min initial rate constants for photodegradations under UV irradiation using post-calcined TiO₂nanofibers after 285° C., 320° C., 360° C., 400° C., 600° C. calcination for 4 hours under ambient atmosphere.

FIG. 6 shows specific surface area measurement of five TiO₂nanofibers with different rutile fraction using Brunauer-Emmett-Teller (BET) method plotted with their initial rate constants during the degradation process as a function of calcination temperature.

FIG. 7 shows a proposed schematic representation of possible electron-hole separation pathway mechanism for anatase and rutile mixed-phase TiO2 nanofibers during the photocatalysis process of PAP.

FIG. 8 shows a schematic image of the photodegradation process on the surface of TiO₂.

FIGS. 9A, 9B and 9C show an EDS spectrum of 5 wt % Pt—TiO₂, showing elemental composition and distribution; a TEM image of TiO₂nanofiber surface decorated with ˜4 nm Pt nanoparticles, and an SEM image of TiO₂nanofibers showing the presence of numerous pores on the titania surface.

FIG. 10 shows a phenazopyridine structure and UV-Vis absorption spectrum showing the progress of phenazopyridine photodegradation with reaction time.

FIG. 11 shows Rhodamine B structure and UV-Vis absorption spectrum showing the progress of Rhodamine B. photodegradation with reaction time.

FIG. 12 shows a schematic representation of the electrospinning process.

FIG. 13 shows an X-ray diffraction profile of TiO₂nanofibers under different temperature calcination for 4 hrs in air.

FIG. 14 shows PMMA/TIP polymer fibers with different diameters under calcination at 359° C. for 4 hrs in air.

FIG. 15 shows a scanning electron microscopy image of calcined TiO₂nanofibers with diameters of 192.4±10.42 nm.

FIG. 16 shows a UV-Vis spectra of PAP solution at T=−60, 0, 75, 120, 180 minutes.

FIG. 17 shows nuclear magnetic resonance of photocatalysis of 100 μM solution of DMMP with P25 nanoparticles in a quartz vial.

FIG. 18 shows nuclear magnetic resonance of photocatalysis of 100 μM solution of DMMP with anatase TiO₂nanofibers in a quartz vial.

FIG. 19 shows the relationship between time and Rh.B concentration percentage.

FIGS. 20A, 20B and 20C show, an SEM image of N3-dye sensitized TiO₂nanofibers (FIG. 20A); a TEM image of N3-dye sensitized TiO₂nanofibers (FIG. 20B); and EDX mapping image of N3-dye sensitized TiO₂nanofibers with purple spots of Ru²⁺(FIG. 20C).

FIG. 21 shows UV-Vis spectra of PAP solution at T=−45, −30, −15, 0, 15, 30, 45 and 60 minutes.

FIG. 22 shows scanning electron microscopy image of platinum nanoparticles supported on electrospun TiO₂nanofibers.

FIG. 23 shows Anatase TiO₂nanofibers, diameter ˜300±50 nm.

FIG. 24 shows ¹³C NMR-Photocatalysis of 2CEES in a nucleophilic solvent with anatase TiO₂nanofibers.

FIG. 25 shows ¹³C NMR-Photocatalysis of 2CEES in an acetone/water solution with anatase TiO₂nanofibers.

FIG. 26 shows photocatalysis of 2CEES in the presence of anatase TiO₂nanofibers without solvent and irradiation in a quartz vial.

FIG. 27 shows photocatalysis of 2CEES in the presence of anatase TiO₂nanofibers without solvent and with irradiation in a quartz vial.

FIG. 28 shows photocatalysis of 2CEES in the presence of water saturated anatase TiO2 nanofibers without solvent and irradiation in a quartz vial.

FIG. 29 shows photocatalysis of 2CEES in the presence of water saturated anatase TiO2 nanofibers without solvent and irradiation in a quartz vial.

FIG. 30 shows ¹³C NMR-Photocatalysis of 2CEES with water saturated TiO₂nanofibers over 24 hours of UV Irradiation.

FIG. 31 shows ¹³C NMR-Photocatalysis of 2CEES with water saturated silica gel over 24 hours of UV Irradiation.

FIG. 32 shows UV-Vis of photocatalysis product after 24 hours of UV irradiation with silica gel.

FIG. 33 shows ¹³C NMR-Hydrolysis study of Dimethylmethyl phosphonate over 72 hours.

FIG. 34 shows ¹³C NMR-Photocatalysis of DMMP with standard Degussa P25 nanoparticles in DI water over 8 hours of UV irradiation.

FIG. 35 shows ³¹P NMR-Photocatalysis of DMMP with anatase TiO₂nanofibers in water over 4 hours of UV irradiation.

FIG. 36 shows photocatalysis of 100 μM solution dimethyl methylphosphonate with anatase TiO₂nanofibers in a 100 mL quartz beaker over 2 hours of UV irradiation.

FIG. 37 shows photocatalysis of 100 μM solution dimethyl methylphosphonate with anatase TiO₂nanofibers in a 16 mL quartz vial over 2 hours of UV irradiation.

FIG. 38 shows TEM imaging of Pt nanoparticles supported on the surface of anatase TiO₂nanofibers.

FIG. 39 shows ³¹P NMR of Photocatalysis with 100 μM solution of dimethyl methylphosphonate and Pt nanoparticles supported on anatase TiO₂nanofibers for 4 hours of UV irradiation.

FIG. 40 shows SEM (above) and TEM (bottom) images of 2 varying diameters of anatase TiO₂nanofibers ranging from 200 to 300 nm in diameter.

FIG. 41A shows the molecular formula of N3.

FIGS. 41B and 41C show UV-VIS spectra of N3 solution and UV-VIS of photodegradation of Phenazopyridine (PAP) using N3-sensitized TiO₂nanofiber (from left to right), respectively.

FIG. 41D shows a Relative wide band gap of TiO₂, which limits its application as photocatalyst using under visible light; N3-dye can absorb visible light and get excited to generate free electrons and transfer to TiO₂, which enlarge the application of TiO₂-based photocatalyst.

FIG. 42 shows photocatalysis of 100 μM solution of dimethyl methylphosphonate with Degussa P25 TiO₂nanoparticles over 4 hours of UV irradiation.

FIG. 43 shows photocatalysis of 100 μM solution of dimethyl methylphosphonate with anatase TiO₂nanofibers over 2 hours of UV irradiation.

FIG. 44 shows Raman spectra of anatase TiO₂nanofibers before and after photocatalysis with DMMP.

FIG. 45 shows an SEM image of blended PMMA/PMMA:TIP polymer fibers.

FIG. 46 shows EDX (mapping) polymer blended nanofibers where blue represents titanium distributed in the matrix.

FIG. 47 shows EDX (mapping) polymer blended nanofibers where green represents oxygen distributed in the matrix.

FIG. 48 shows EDX (mapping) polymer blended nanofibers where red represents the carbon distributed in the matrix.

FIG. 49 shows ³¹P NMR of the photodegradation of 100 μM DMMP with TiO₂nanofibers.

FIGS. 50A and 50B show that the degradation process is a first-order reaction; Anatase/RGO has a higher initial rate constant (k=0.0384 min⁻¹) than pure anatase nanoparticles (k=0.0301 min⁻¹) during the first 30 mins degradation.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Certain exemplary embodiments of the present invention will now be described in greater detail with reference to the accompanying drawings.

TiO₂nanofibers were prepared with different rutile fractions ranging from 3 wt % to 97 wt % by adjusting their calcination temperature.

These materials were applied to the photocatalytic degradation of a model pharmaceutical agent, phenazopyridine [2,6-diamino-3-(phenylazo)pyridine hydrochloride, (PAP)], which is used commercially as an analgesic for urinary tract infections [37, 38]. Physical characterization combined with determination of initial degradation rate constants provided insight to the mechanism and optimization of these new materials for decontaminating toxic pharmaceutical agents in water.

##STR00001##

Example 1

Polymethylmethacrylate (PMMA) (M_w960,000), titanium isopropoxide (TTIP), N,N-dimethylformamide (DMF), chloroform and phenazopyridine hydrochloride (PAP) (M_w249.70) were all acquired from Sigma Aldrich and used as received.

1 2 mL of PAP solution with concentration of 144 μM was prepared using DI water as solvent. The solution was transferred into a 16 mL cylindrical quartz container and placed in a fume hood with the lights off. After blanking the UV-Vis Spectrophotometer with DI water in a small quartz cell, an initial reading (marked as T=−60) was taken by diluting 0.5 mL of the PAP solution with 2.0 mL of DI water. Next, 12.0 mg of the catalyst TiO₂nanofibers were added into the 12 mL PAP solution with constant stirring. After 30 and 60 minutes stirring, a 1.0 mL aliquot of the sample was taken and centrifuged for two minutes, which are recoded as sample T=−30 and T=0. Once the sample of T=0 was taken, a UV lamp was turned on at a fixed distance of 9 cm from the center of the quartz cell and 1.0 mL aliquot of the sample was took every 10 minutes and centrifuged for two minutes. Once the centrifuging was complete, 0.5 mL of the upper solution from the mixture was taken off from the top of the sample and diluted with 2 mL of DI water. The diluted sample was run through the UV-Vis Spectrophotometer and an absorbance spectrum was obtained at T=10, 20, 30, 45, 60.

The electrospun pre-calcined polymer fibers were fabricated using a high voltage Spellman SL 30 generator, where a high electrical potential was applied across the syringe needle attached to a copper wire and the collector screen. The photodegradation experiments were performed using an Oriel 66001 UV lamp with Oriel 68805 40-200 Watt universal Arc lamp power supply, which covered all the UV ranges. The distance between the center of the solution container and the UV lamp was controlled at 9 cm. UV-Visible analysis of the aliquots was performed on an 8452A Hewlett Packard Diode Array spectrophotometer instrument with wavelength from 190 nm to 820 nm to characterize the absorption spectra of the aliquots to determine the phenazopyridine concentration changes and also to identify the degradation products. Sample analyses were performed in distilled water unless otherwise noted. The morphological and structural characteristics of the pre-calcined polymer and after-calcined TiO₂nanofibers were measured by field emission scanning electron microscopy (FESEM, Supra 55 VP from Zeiss equipped with an EDAX energy dispersive X-ray spectroscopy detector), and X-ray diffraction (XRD, PANalytical's X'Pert PRO Materials Research Diffractometer with Cu Kα radiation (λ=1.5418 Å)) respectively. Specific surface area of the samples was measured by Brunauer-Emmett-Teller (BET) method using a surface analyzer.

TiO₂nanofibers were prepared by a typical sol-gel synthesis followed by electrospinning technique and calcination treatment shown in the schematic FIG. 1. A polymeric sol-gel was generated by stirring and hydrolysis of TTIP using 1:2 mass ratio of PMMA:TTIP, where 320 mg of PMMA was dissolved in 2 mL chloroform followed by drop wise addition of 640 mg of TTIP with continuous stirring. 2 mL DMF was then added to increase the dielectric constant of the composite solution required for the electrospinning. The high voltage would pull the precursor sol-gel from the syringe onto the conductive collector forming polymer nanofibers. The resulting polymer fibers were left overnight to allow for complete hydrolysis of TTIP to TiO₂followed by heat calcination for transformation from amorphous phase to crystal phases. By adjusting the calcination temperatures from 285° C. to 600° C., TiO₂nanofibers with different composition fractions of anatase phase and rutile phase can be fabricated under ambient atmosphere for 4 hours.

FIG. 2 presents six SEM images of pre-calcined polymer fibers and the post-calcined TiO₂fibers followed by calcination after 285° C., 320° C., 360° C., 400° C. and 600° C. for 4 hours under ambient atmosphere. As shown, TiO₂nanofibers after calcination at 285° C., 320° C., 360° C. and 400° C. all had folded surface morphology. And their average diameters didn't change much compared with the pre-calcined polymer fibers shown in table 1. When the temperature increased to 600° C., the morphology of the fibers was obviously different and the diameter shrank a lot. It also showed much smoother surface with a larger grain size from the surface observation.

TABLE 1

Samples prepared under different temperature calcination showing
different diameters, rutile fractions and grain sizes.
					Rutile
Sample	Calcination		Rutile	Anatase	Phase
in SEM	temperature	Diameter	Fraction	Phase Grain	Grain Size
image	(° C.)	(nm)	(%)	Size (nm)	(nm)

A	N/A	761.6 ± 40.3	N/A	N/A	N/A
B	285	666.0 ± 43.8	8	16.77	33.68
C	320	720.5 ± 40.3	16	11.18	15.55
D	360	676.5 ± 60.0	38	13.41	22.45
E	400	685.3 ± 42.4	67	16.77	25.26
F	600	441.2 ± 41.4	97	50.25	33.68

The XRD patterns of post-calcined TiO₂nanofibers at 285° C., 320° C., 360° C., 400° C. and 600° C. with 4 hours holding times under ambient atmosphere are shown in FIG. 3. The “A” and “R” in the figure denoted the anatase and rutile phases, respectively. Well defined diffraction peaks for the post-calcined TiO₂nanofibers suggested the presence of both anatase and rutile phases. For anatase phase, the major peaks were obtained at 2 theta values of 25.5°, 37.9°, 48.2°, 53.8°, and 55.0° representing the Miller indices of (101), (004), (200), (105), and (211) planes, while for rutile peaks were observed at 27.6°, 36.10, 41.2°, and 54.30, which correspond to the Miller indices of (110), (101), (111), and (211) planes. It was clearly seen that with increasing calcination temperature, the intensities ratio between the rutile phase and the anatase phase increased simultaneously. The weight fraction of anatase-to-rutile transformation in the post-calcined TiO₂nanofibers can be calculated from the equation W_R=1/[1+0.8(I_A/I_R)][19, 26, 27], where I_Ais the X-ray integrated intensities of the (101) reflection of anatase around 25.5° and I_Ris that of the (110) reflection of rutile around 27.6°. The fraction of rutile phase in TiO₂nanofibers was found to increase with increasing calcination temperature from 8% to 97% shown in table 1. Almost pure rutile nanofibers can be prepared around 600° C. calcination for 4 hours under ambient atmosphere.

According to Scherrer Equation based on XRD pattern in FIG. 3, the grain sizes of anatase and rutile phase can be calculated and are listed in Table 1. When calcination temperature increased, the size of anatase and rutile grains increased as well as the rutile fractions. It suggested that the transformation from anatase to rutile phase and the grains growth happened at the same time.

In order to study the influence of rutile fraction in TiO₂nanofiber on the photodegradation activities, six degradation experiments with and without using nanofibers with different rutile fractions were performed under the same condition. 144 μM of PAP solution was used as the initial pollutant for photodegradation. Based on the UV-Vis absorbance peak changes at 428 nm, the PAP concentration changes both in the dark and under UV irradiation were plotted as a function of time shown in FIG. 4. Pure PAP solution without any catalysts was very stable regardless of whether it is maintained in the dark or subjected to UV irradiation. As the weight fraction of rutile phase increased from 8% to 38%, the photodegradation activity of the TiO₂nanofibers improved. However, further increase of the rutile fraction led to a slower degradation activity. All PAP solution could be completely degraded in 45 minutes by using the TiO₂nanofibers with 38 wt % of rutile.

Based on FIG. 4, the data were best fit under pseudo-first-order reaction. The rate constant and the kinetic equation can be expressed as C=C₀e^−kt, where t is the reaction time; k is the rate constant; C₀and C are the PAP initial concentration and concentration at reaction time of t, respectively. The initial rate constant k during the first 30-min degradation period using five TiO₂nanofibers with different rutile fractions were calculated and plotted with the rutile fractions together as a function of calcination temperature shown in FIG. 5. It was clear that the initial rate constant of TiO₂nanofibers strongly depends on the rutile fraction in the nanofibers, which could be tuned through the calcination temperature. The optimal initial rate constant was 0.044 min⁻¹using TiO₂nanofibers with 38 wt % of rutile after calcination at 360° C. for 4 hours under ambient atmosphere.

TiO₂nanofibers with 38 wt % of rutile phase exhibited the best initial rate constant during the PAP degradation process. Specific surface area of the five TiO₂nanofibers was measured by Brunauer-Emmett-Teller (BET) method. The result showed us that, as the rutile fraction increased, the surface area of the TiO₂nanofibers decreased, which suggested that the TiO₂nanofibers with higher fraction of rutile phase had a lower surface area. If other factors are not considered, higher surface area would leave more active sites for H₂O and O₂adsorbed on the surface for the generation of more active radicals to get a better degradation initial rate constant. TiO₂nanofibers with higher surface area have a better initial rate constant. FIG. 6 shows that the TiO₂nanofibers with 38 wt % of rutile and surface area of 22 m²/g had the best initial rate constant of 0.044 min⁻¹rather than 8 wt % rutile nanofibers with higher surface area of 108 m²/g got the best initial rate constant. Therefore, it appears that surface area is not the only factor determining the photoactivity efficiency.

FIG. 7 shows a proposed schematic representation of possible electron-hole separation pathway mechanism for anatase and rutile mixed-phase TiO₂nanofibers during the photocatalysis process of PAP.

Rutile fraction difference is believed to be another factor leading to the different initial rate constants. During the calcination process, amorphous phase TiO₂was firstly going to transfer to anatase phase at a relative lower temperature. As the calcination kept going, small anatase crystal would like to grow to a bigger one. The photocatalytic activity principle of anatase and rutile mix-phase TiO₂nanofibers is hypothesized as shown in FIG. 7. Recently a new understanding of the band alignment between rutile and anatase showed that the electron affinity of anatase was higher than rutile and the conduction electrons would flow from rutile to anatase [39], which helped to explain the electron-hole separation during the photodegradation process of PAP. As shown in FIG. 7, between anatase and rutile phases, the photoexcited electrons would migrate from conduction band of rutile to conduction band of anatase. Meanwhile, the electrons in the valence band of rutile also tended to migrate into valence band of anatase. This electron transfer process could also be regarded as the holes transportation from anatase to rutile. This whole process made the excited electron-hole pairs exist separately in the conduction band of anatase and valence band of rutile. This would effectively increase the charge separation, decrease the electron-hole pair recombination and consequently improve the photocatalytic efficiency of the post-calcined TiO₂nanofibers. The electrons and holes were going to separately react with surface adsorbed H₂O and O₂to generate active hydroxyl radicals and superoxide radical anions. These oxidizing radicals would consequently react with PAP and decompose it into some other smaller molecules. During this process, oxygen-hydrogen bond in H₂O was going to break and electrons would migrate into valence band of rutile to replenish the excited missing electrons making the nanofibers reusable.

As the calcination temperature increased, more rutile phase showed up in the post-calcined TiO₂nanofibers. This change made the surface area of post-calcined TiO₂nanofibers decrease. Theoretically, the initial rate constant would decrease as a result of decreased specific surface area. However, more rutile phase in the post-calcined TiO₂nanofibers would help to improve the electron-hole pair separation to increase the initial rate constant. These two factors competed with each other making the 38 wt % of rutile fraction TiO₂nanofibers have the best initial rate constant.

TiO₂nanofibers with different rutile fractions ranging from 3 wt % to 97 wt % were successfully synthesized by sol-gel method followed by electrospinning and calcination at different temperatures under ambient atmosphere. As the calcination temperature increased, the rutile fraction in TiO₂nanofibers increased as well, however the surface area showed an opposite trend. The photocatalytic activity showed that post-calcined TiO₂nanofiber calcined at 360° C. containing 38 wt % of rutile got the highest initial rate constant and the fastest degradation efficiency. 144 μM PAP could be completely removed in 45 mins. The existence of an optimum rutile fraction in TiO₂nanofiber can be explained by the competition between less surface area decreasing the generation of radicals and appropriate amount of rutile phase leading to more efficient electron-hole separation and more generation of radicals. 38 wt % rutile TiO₂nanofibers provided a new type of material for the future application in the pharmaceutical waste treatment and other environmental remediation.

Example 2

Nanotechnology can provide new approaches to the real time decontamination of liquids and solid surfaces. For example, photocatalytic and self-cleaning ability on the hydrophilic surface of TiO₂have found multiple uses in health, environmental and military applications. Specifically, TiO₂-based electrospun fibers have great potential for use in chemical and biological decomposition [44], protective/self-cleaning clothing [40, 45], self-cleaning glass [46], and self-cleaning membranes.[47] The basic principle of photocatalytic activity is the use of incident light to excite an electron from the valence band (leaving behind a hole) to the conduction band of a semiconductor. These photoinduced charge carriers then proceed to form reactive radicals, hydroxyl radicals (A−) and super oxide radicals (D+) that attack adsorbed chemicals on the surface of the material, as shown in FIG. 8, which shows a schematic image of the photodegradation process on the surface of TiO₂. Previous research on titania modified textiles has concentrated on increasing the number of hydroxyl and carboxyl radicals on the surface of the fiber. [48-49].

Major setbacks in this area of research are the low surface-volume ratios, limiting adsorption capability and photocatalytic activity, and the use of UV light for photo-excitation, which prevents the use of low intensity of typical indoor working conditions. Our objective is to use the electrospinning technique to fabricate TiO₂fibers with large surface area for heterogeneous catalysis. [50, 51]

FIGS. 9A-9C shows FIG. 9A: EDS spectrum of 5 wt % Pt—TiO₂, showing elemental composition and distribution. FIG. 9B: TEM image of TiO₂nanofiber surface decorated with ˜4 nm Pt nanoparticles. FIG. 9C: SEM image of TiO₂nanofibers showing the presence of numerous pores on the titania surface.

FIG. 10 shows a UV-Vis absorption spectrum showing the progress of phenazopyridine photodegradation with reaction time.

In addition to metal nanoparticles supported on TiO₂nanoparticles, high surface area graphene nanoparticles may be incorporated into the TiO₂anatase crystallites for increased absorption and diffusion of reactants within the TiO₂surface. Graphene's increased electron conductivity is expected to modify TiO₂'s electronic, crystal and surface structures to allow the application of low intensity room lighting for the decontamination of organic pollutants. Preliminary studies have shown successful degradation of phenazopyridine, a pharmaceutical drug, using low intensity room lighting.

FIG. 11 shows Rhodamine B Structure, and UV-Vis absorption spectrum showing the progress of Rhodamine B. photodegradation with reaction time. Further investigation into the varying forms of carbon such as amorphous carbon can potentially be said to have an improvement on decontamination of organic pollutants. The presence of amorphous carbon in and throughout the surface of titania will not only increase the surface area but expand the pore size allowing for functionalization. Initial studies have shown promising initial rates of degradation of Rhodamine B. in ultra-violet irradiation. Using the polyol synthesis to deposit noble metals [51] on the surface of TiO₂-AC (Amorphous Carbon) metals such as platinum can be used as an anchor for metal organic frameworks for degradation. If successful, the technology and materials developed in this work have the potential to be utilized in environmental decontamination from chemical and biological contaminants, tissue engineering, drug delivery and clothing/textile self-cleaning applications.

Huge amounts of environmental toxins, such as toxic industrial chemicals (TICs), toxic organic dyes, bio-pharmaceuticals, and chemical warfare agents (CWAs), bio-accumulate causing chronic and aesthetic pollution to the surrounding environments and human beings. Systems must therefore be put in place for treatment methods that ensure complete degradation (with no secondary pollution) before being released into the environment. Compared with other photocatalytic materials, one-dimensional metal oxide nanofibrous materials have attracted considerable attention due to their high specific surface area, ease of fabrication and functionalization, and versatility in controlling the fiber diameter and morphology. Electrospun nanofibers from stable polymers are ideal candidates for catalytic supports as they can provide a large surface area and a high porosity for catalytic applications. In order to develop novel self-cleaning surfaces and substrates for photodegradation of environmental toxins, some fundamental studies have been investigated on the electrospinning technique, calcination temperature influence on TiO₂phase changes and phase transformation rates of pre-calcined polymer fibers with different diameters. We have prepared a variety of electrospun nanofibrous materials such as, anatase TiO₂, rutile TiO₂, reduced graphene oxide TiO₂, BaTiO₃, platinum nanoparticles supported on anatase TiO₂, ZnO, photoactive dye supported anatase TiO₂. These fibers have been characterized by X-Ray diffraction, Scanning Electron Microscopy, Transmittance Electron Microscopy, Raman Microscopy and Energy-Dispersive X-Ray Spectroscopy. Also, electrospun TiO₂nanofibers show excellent UV degradation results on Rhodamine B (Rh.B.), phenazopyridine (PAP) and dimethyl methylphosphonate (DMMP). The photocatalytic activity of pure TiO₂fibers is limited by fast electron-hole pairs' recombination and a relative high energy band gap. Some multifunctional TiO₂fibers have been also fabricated to solve these problems. These novel multifunctional materials offer excellent mobility of charge carriers for faster degradation and the possibility to exploit catalytic processes in decontamination.

For synthesis procedure, sol-gel method is used to get the pre-electrospinning solution. A 1:2 weight ratio of polymethylmethacrylate (PMMA):titanium isopropoxide (TIP) was prepared by completely dissolving PMMA in chloroform followed by drop wise addition of TIP with continuous stirring of the reaction mixture for complete dissolution. Small amount of dimethylformamide (DMF) was added to increase the dielectric constant of the composite solution and hence enable the electrospinning process at a high voltage. The hydrophobic nature of both PMMA and TIP enabled the formation of a homogeneous solution of the polymer blend. Electrospinning is a non-mechanical, electrostatic process that produces fibers in the nanometer to micrometer range using electrically driven jets of polymer solution. 15-40 kV was applied across the syringe needle and the collector screen where the PMMA/TIP solution was spun into composite nanofibers and deposited as a randomly oriented non-woven mat on the collector screen. These polymer fibers were left overnight to undergo hydrolysis reactions, followed by thermal treatment in order to favor structural stability via sintering, densification, grain growth and phase transformation.

Example 3

FIG. 12 shows a schematic representation of the electrospinning process Calcination temperature influence on TiO₂phase changes. Based on the calcination temperatures, TiO₂nanofibers show different phase combination, pure anatase, pure rutile or their mixture. The X-ray diffraction (XRD) in FIG. 13 clearly shows that pure anatase phase of TiO₂shows up at relative lower temperature and it begins to transfer to rutile phase as the temperature increases. The ratios of anatase phase and rutile phase under different temperature are shown in table 1.

TABLE 2

Polymer nanofibers with different diameters prepared
under different electrospinning parameters
				Distance
PMMA/TIP			PMMA	between Tip to
Polymer	Diameter	PMMA:TTIP	Molecular	Collector	Voltage
Fiber	(nm)	(mg)	Weight	(cm)	(kV)	Humidity

A	638.4 ± 26.3	320:640	996,000	18	25	43%
B	761.6 ± 40.3	320:640	996,000	11	25	85%
C	972.8 ± 134.8	320:640	996,000	11	25	43%

PMMA/TIP polymer fibers with different diameters can be fabricated by altering the parameters used in sol-gel preparation and electrospinning process as shown below in Table 2. As shown in Table 2, humidity is and tip distance both influence fiber diameter.

FIG. 13 shows X-ray diffraction profile of TiO₂nanofibers under different temperature calcination for 4 hrs in air.

As shown in FIG. 14, under the same calcination condition polymer fibers with larger diameters have a faster anatase to rutile transformation rates and larger grain sizes.

TABLE 3

Calcination temperature vs. anatase/Rutile phase fraction
Calcination	Anatase Phase	Rutile Phase
Temperature (° C.)	Fraction (%)	Fraction (%)

325	100	0
400	85	15
465	74	26
580	61	39
600	0	100

Table 3 shows the phase fraction of anatase and rutile in TiO₂nanofibers under different temperature calcination.

FIG. 14 shows PMMA/TIP polymer fibers with different diameters under calcination at 359° C. for 4 hrs in air Photodegradation of PAP using electrospun TiO₂nanofibers under UV light. TiO₂nanofibers with diameter of 192.4±10.42 nm were fabricated and utilized as the photocatalyst in degradation of PAP solution, as shown in the scanning electron microscopy image in FIG. 15. Firstly, stir PAP solution with catalyst in the dark for 60 mins to ensure adsorption/desorption equilibrium, extract 0.5 ml upper solution and dilute in 3 ml DI water to run UV-Vis analysis (T=−60, 0). Then turn on UV lamp, continue stirring the solution and pick up mixture solution, centrifuge, extract upper solution and dilute after 75 mins, 120 mins and 180 mins irradiations. FIG. 16 shows a UV-Vis spectra of PAP solution at T=−60, 0, 75, 120, 180 minutes. Photodegradation of DMMP using electrospun TiO₂nanofibers under UV light. From UV-Vis spectra in FIG. 16, it can be concluded that the concentration of PAP solution start to decrease after turning on the light. After 120 mins irradiation, almost all the PAP are degraded. At T=180 mins, new product peak is generated.

FIG. 17 shows nuclear magnetic resonance of photocatalysis of 100 μM solution of DMMP with P25 nanoparticles in a quartz vial. FIG. 18 shows nuclear magnetic resonance of photocatalysis of 100 μM solution of DMMP with anatase TiO₂nanofibers in a quartz vial. The multifunctional TiO₂fibers-TiO₂/Reduced Graphene Oxide (RGO) Nanofibers result in photodegradation of Rh.B under visible light. As shown below in FIGS. 17 and 18, the degradation of DMMP using TiO₂nanofibers is much faster than using P25 nanoparticles that the DMMP peak disappears in 2 hrs using TiO₂nanofibers while it took 4 hrs using P25 nanoparticles.

FIG. 19 shows that TiO₂/RGO nanofibers have a faster degradation rate than any other catalyst for photodegradation of Rh.B. under visible light. The best mass ratio between TiO₂and RGO is still under study.

FIG. 20 shows, Left to right: SEM image of N3-dye sensitized TiO₂nanofibers; TEM image of N3-dye sensitized TiO₂nanofibers; EDX mapping image of N3-dye sensitized TiO₂nanofibers with purple spots of Ru²⁺. As seen in SEM image in FIG. 20, N3 dyes are attached on the surface of TiO₂nanofibers. After soaking TiO₂and N3 dye together in NaOH solution, the N3 dye was able to bond to the TiO₂nanofibers. N3-sensitized TiO₂nanofibers were confirmed by using SEM, TEM and EDX mapping techniques.

FIG. 21 shows UV-Vis spectra of PAP solution at T=−45, −30, −15, 0, 15, 30, 45 and 60 Novel multifunctional TiO₂fibers—platinum nanoparticles supported on electrospun TiO₂nanofibers. In FIG. 21, it shows that there is no PAP solution UV-Vis absorbance change when stirring in dark. After turning on the lamp, PAP absorbance peak starts to decrease, which shows the degradation process happens. FIG. 22 shows a scanning electron microscopy image of platinum nanoparticles supported on electrospun TiO₂nanofibers. Platinum nanoparticles supported on electrospun TiO₂nanofibers have faster electron-hole pairs separation and an improved degradation efficiency as compared to electrospun TiO₂nanofibers.

TABLE 6

Potential Target Pollutants.
		Simulated Chemical
Toxic Industrial	Abbrevi-	Warfare	Abbrevi-
Chemicals (TICS)	ation	Age_nts (SCWAs)	ation

Ammonia	NH₃	2-Chloro ethyl ethyl sulfide	CEES
Arsine	AsH₃	Dimethyl methylphosphonate	DMMP
Boron trifluoride	BF₃	Dimethyl chlorophosphate	DMCP
Carbon disulfide	CS₂	Diisopropyl fluorophosphates	DIFP
Formaldehyde	CH₂O	O,O-Dimethyl O-(4-	Methyl
		nitrophenyl) phosphate	Paraoxon
Hydrogen cyanide	HCN
Hydrogen sulfide	H₂S
Phosgene	COCl₂
Sulfur dioxide	SO₂
Carbon monoxide	CO
Methyl bromide	CH₃Br
Nitrogen dioxide	NO₂
Phosphine	PH₃
Cyanogen	ClCN
chloride

The following types of agents may be degraded by the catalytic fiber:

Toxic organic dyes: Rhodamine B, Methyl Yellow, Methyl Red, etc.

Bio-pharmaceuticals: Phenazopyridine, etc.

Chemical warfare agents (CWAs): O-Pinacolyl methyl phosphonofluoridate (GD), (RS)-Propan-2-yl methylphosphonofluoridate (GB), (RS)-Ethyl N,N-Dimethylphosphoramidocyanidate (GA), Ethyl ({2-[bis(propan-2-yl)amino]ethyl}sulfanyl)(methyl)phosphinate (VX), bis(2-chloroethyl) sulfide (HD), 2-Chloroethyl Ethyl Sulfide, etc.

The photocatalytic fibers may be used for the following purposes:

Nanofibrous membranes for water purification treatment. Functionalized nanofibrous membranes can be used for remediation of wastewaters under visible light atmosphere

Air or gas filtration used in gas mask. Air filtration is conventionally performed by fibrous filters primarily due to their high collection efficiency also durability. The very high surface area facilitates adsorption and degradation of contaminants from air.

Protective clothing for chemical warfare agents. Chemical warfare agents in the battlefields are usually in the form of aerosol or vapors. Hence, protective systems such as clothing and face masks are highly needed to safeguard the people from an eventual chemical or biological hazard. Metal oxide nanofibrous mats can be applied into suitable protective clothing which is adaptability with the physiological conditions of the human body acting as a barrier against toxic and unwanted materials, such as aerosol particles, harmful vapors, and liquids.

One important discovery was found that for pre-calcined polymer fibers with different diameters, different rutile fractional crystal phase titanium fibers can be fabricated after the same calcination condition treatment and results in modification of the photocatalytic activity.

Over the past few years, it has been demonstrated that the electrospun titania nanofibers provide a faster photodegradation rates of Rhodamine B (Rh.B.), phenanzopyridine (PAP) and dimethyl methylphosphonate (DMMP) compared to conventional TiO₂nanoparticles. Besides that, many strategies have been also developed to fabricate several multifunctional nanofibrous materials to enhance their photocatalytic performance, among which photoactive dye supported anatase TiO₂and reduced graphene oxide TiO₂shows an excellent performance of degradation of Rh.B. and PAP under visible irradiation. These novel multifunctional materials offer excellent mobility of charge carriers for faster degradation and the possibility to exploit catalytic processes in real time decontamination.

Poly(3,4-ethylenedioxythiophene) or PEDOT is a conducting polymer based on 3,4-ethylenedioxythiophene (EDOT) monomer. It is transparent, and generally has high stability, a moderate band gap and low redox potential. PEDOT can be electrogenerated directly on a conductive support (Pt, Au, glassy carbon, indium tin oxide, . . . ) in organic solvents or in aqueous solution. In one study [Zhang, Xinyu; MacDiarmid, Alan G.; Manohar, Sanjeev K. (2005). “Chemical synthesis of PEDOT nanofibers”. Chemical Communications (42): 5328-30. doi:10.1039/b511290g. PMID 16244744] PEDOT nanofibers are produced from vanadium pentoxide nanofibers by a nanofiber seeding method. In this procedure EDOT is dissolved in an aqueous solution of camphorsulfonic acid (CSA) and a vanadium pentoxide nanofiber sol-gel and radical cationic polymerization is initiated by addition of ammonium persulfate. The resulting polymer precipitates from solution and has a general composition (PEDOT)(CSA)0.11-(HSO4)0.12(Cl)0.11(H2O)0.19. Washing with dilute hydrochloric acid removes the vanadium compound. The presence of the vanadium pentoxide seeds are believed to make the difference between the formation of PEDOT nanofibers (100 to 180 nanometer diameter and one to several micrometres long) and the formation of a more conventional granular morphology.

TABLE 7

	Phase Composition
Initial Metal	(Rutile Fraction
Oxide	with the balance
Materials	of Anatase)	Materials Compositions

TiO₂	8%	TiO₂-MOF Nanofibers
Nanofibers
ZnO	16%	TiO₂-PEDOT Nanofibers
Nanofibers
	38%	TiO₂—N₃dye Nanofibers
	67%	TiO₂-Reduced Graphene Oxide
		Nanofibers
	97%	TiO₂—Pt Nanofibers
		TiO₂—Pd Nanofibers

Example 4

Electromagnetic radiation in the form of visible light, ultra-violet light, or even sunlight can be used to achieve enhanced photodegradation of CWAs that are both rapid and inexpensive compared to the current decomposition techniques that are costly and time consuming. This program aims to take advantage of advances in the fabrication of nanofibers activated by visible irradiation for targeted decontamination of CWAs—technology which can be used for the improvement of gas masks, for integration with conventional textiles for self-decontaminating garments, and for spray treatments of combat vehicles.

The protection of the warfighter against chemical warfare agents (CWAs) and other biological and environmental toxins is essential on the modern battlefield. Nanotechnology can provide novel systems for rapid decontamination and protection through a self-cleaning mechanism. Electromagnetic radiation in the form of visible light, ultra-violet light, or even sunlight can be used to achieve enhanced photodegradation of CWAs that are both rapid and inexpensive compared to the current decomposition techniques that are costly and time consuming. This technology takes advantage of nanofibers activated by visible irradiation for targeted decontamination of CWAs, technology which can be used for the improvement of gas masks, for integration with conventional textiles for self-decontaminating garments, and for spray treatments of combat vehicles.

The production of electrospun titania nanofibers provides an increase in surface area that elicits faster decomposition compared to conventional TiO₂nanoparticles. Self-assembled Metal Organic Frameworks (MOFs) may be combined with doped catalysts onto the titania, such as platinum, and used to further increase the rate of degradation. Introduction of noble metals to semiconductors permits creation of a rapid exchange of electrons to the electrolyte, improving the electronic properties of the catalyst. In addition, new tubular structures will be explored. A related but alternate approach is the production of structures such as zirconia and zinc oxide as approaches to increase the overall efficiency of decontamination.

TiO₂nanofibers represent an alternative approach to conventional composites for use in photocatalytic degradation. The one dimensional morphology of TiO₂is desired compared to spherical TiO₂nanoparticles; owing to excellent mobility of charge carriers, high surface area, the existence of pores enhancing the accessibility of electrodes to the hole transporting materials and hence enhanced charge collection and transport.

The nanofibrous materials were synthesized via a polyol synthesis, where platinum nanoparticles were deposited on TiO₂nanofibers, or with carbonaceous or graphitic materials. These were confirmed by EDX analysis, See FIG. 9A. The purpose of the modified catalyst was to affect the band gap energy of the TiO₂, a lower energy would result in visible light exciting an electron from the conduction band to the valence band rather than ultraviolet irradiation.

Preliminary photocatalysis and degradation using the new materials was achieved utilizing in aqueous and non-aqueous solutions. Due to the toxicity and availability of chemical warfare agents, chemical analogs were used as an alternative. One common simulated chemical warfare agent (SCWA) of interest, 2-Chloroethyl ethyl sulfide, an analog for mustard gas, undergoes a hydrolysis mechanism in the presence of water. Therefore, it became difficult to determine if the degradation was occurring due to the radicals present in solution from the catalyst or the hydrolysis from the water, see FIGS. 24-27.

Photocatalysis experiments were modified to accommodate the necessary UV irradiation by performing the experiments in a quartz reaction vial. In previous experiments glass vials were being used as a reaction vessel however, for TiO₂to be a catalyst in photodegradation, electron-hole pairs must be formed. Without the energy of UV irradiation this becomes nearly impossible and therefore, no degradation will occur.

Dimethyl methyl phosphonate, a simulated chemical warfare agent for Sarin is being studied as a toxic pollutant. Preliminary studies showed DMMP was not susceptible to hydrolysis and therefore would be a better candidate for photocatalysis studies with TiO₂nanofibers. Results of the photocatalysis of DMMP with TiO₂nanofibers showed degradation of the pollutant in a one hour time span where TiO₂nanoparticles resulted in a 4 hour degradation time span, FIGS. 45 and 49. This also proved that nanofibers were better than nanoparticles and that surface to volume ratio plays a larger role in the photocatalytic degradation process than the surface area of nanoparticles.

All photocatalysts use incident irradiation in the UV or visible region of the spectrum to excite an electron from the valence band (leaving behind a hole) to the conduction band of a semiconductor. These photoinduced charge carriers then proceed to form reactive radicals, hydroxyl radicals (A−) and super oxide radicals (D+) that attack adsorbed chemicals on the surface of the material, FIG. 8.

The electrospinning procedure may employ a sol gel solution in a 1:2 ratio of polymer to inorganic precursor, polymethylmethacrylate to titanium isopropoxide. A high voltage (25 kV/cm) is applied to the sol gel polymer solution. The sol gel is pulled through a metal needle as an electrified jet which collected on the counter electrode. The solvent evaporates as the fiber mat is deposited. Upon hydrolysis of the fiber mat will undergo a calcination process under thermally controlled atmospheric conditions producing the desired crystal structure of TiO₂. At 400 centigrade for 4 hours anatase TiO₂nanofibers were produced, as shown in FIG. 23, which shows Anatase TiO₂nanofibers, diameter ˜300±50 nm.

Due to the toxicity and availability of chemical warfare agents, chemical analogs will be used as an alternative. One common simulated chemical warfare agent (SCWA) of interest, 2-Chloroethyl ethyl sulfide, an analog for mustard gas, undergoes a hydrolysis mechanism in the presence of water. Preliminary studies have led to degradation experiments utilizing the fabricated catalyst in aqueous and non-aqueous solutions. ¹³C NMR was used to examine the results of the degradation.

FIG. 24 shows ¹³C NMR-Photocatalysis of 2CEES in a nucleophilic solvent with anatase TiO₂nanofibers. In the presence of catalyst and a non-nucleophilic solvent such as acetone the 4 characteristic peaks of 2-CEES were unaffected by the catalyst and UV irradiation. Resulting data was conducive with our knowledge and hypothesis that water will play a role in the degradation mechanism. Upon completion of degradation studies of varying non-nucleophilic solvents the experiments led to a 50:50 solution of water and acetone. 2-CEES may have some interaction with the water in the form of hydrolysis as well as the TiO₂acting as a catalyst for further degradation.

FIG. 25 shows ¹³C NMR-Photocatalysis of 2CEES in an acetone/water solution with anatase TiO₂nanofibers. After standard experiments were done catalyst was added to the solution and the experiment was repeated. Minimal changes to degradation were seen in the presence of anatase TiO₂nanofibers. The presence of absorbed water is detrimental for the efficient use of TiO₂nanofibers as a catalyst.

After studying 2-Chloroethethyl sulfide in a variety or nucleophilic and non-nucleophilic solvents the experimental procedure was altered to a solvent-less system, where extractions in acetonitrile-d3 were done for ¹³C NMR analysis. Below are the results pertaining to a degradation of 2-Chloroethyl ethyl sulfide with anatase TiO₂nanofibers.

FIGS. 26 and 27 show results for photocatalysis of 2CEES with anatase TiO₂nanofibers, without solvent, in a quartz vial. No change was seen over a twenty four hour period. The reaction mechanism of TiO₂was analyzed and showed that without the presence of absorbed water and oxygen, degradation would not occur. After the separation of electron-hole the absorbed water and oxygen will react the negative electron and positive hole creating superoxide and hydroxyl radicals. It is the presence of these radicals that initiate the degradation process. It is understood that 2-Chloroethyl ethyl sulfide hydrolyzes readily in water therefore it was necessary to be able to differentiate between the hydrolysis of 2-Chloroethyl ethyl sulfide and photodegradation. This led to an experiment where the TiO₂nanofibers were soaked in deionized water for 1 hour and excess water was removed prior to the addition of 2-Chloroethyl ethyl sulfide.

FIGS. 28 and 29 show photocatalysis of 2CEES in the presence of water saturated anatase TiO₂nanofibers without solvent, without and with UV irradiation in a quartz vial. After twenty four hours of UV irradiation, the 2-CEES completely degrades into its hydrolysis products where the sample being kept in the dark has no change over the same twenty four hour period.

FIGS. 30 and 31 show ¹³C NMR-Photocatalysis of 2CEES with water saturated TiO₂nanofibers and silica gel over 24 hours of UV Irradiation. The resulting peaks after 24 hours of UV irradiation are consistent with peaks of 2CEES hydrolysis making it uncertain if TiO₂is playing a role in the hydrolysis process. Therefore, a control experiment was performed where silica gel replaced the TiO₂in the photocatalysis and the experiment was repeated.

It was surprising to see a change in 2-Chloroethyl ethyl sulfide while in the presence of silica gel. After 24 hours not only was there a change in the ¹³C NMR but also a visible change in color, from clear to pale yellow. UV-Vis spectroscopy was performed on the final product. The sample was sealed and frozen for GC-MS analysis at a later date. Silica gel was also sent to ECBC for breakthrough testing.

FIG. 32 shows a UV-Vis analysis of photocatalysis product after 24 hours of UV irradiation with silica gel.

A 1 M solution was prepared of dimethyl methyl phosphonate in water. An aliquot was analyzed after hours 1, 4, 8, 24 and 72. The ¹³C NMR showed no change after a 72 hour time period.

FIG. 33. shows a ¹³C NMR-Hydrolysis study of Dimethylmethyl phosphonate over 72 hours. A control experiment was performed using standard Degussa P25 nanoparticles after 72 hours of UV irradiation yielded no change in the presence of anatase TiO₂nanofibers. Experimental conditions remained the same as previous trials the only changing variable was the shape of the catalyst. Concentration of solution remained constant at 1 M. After an 8 hour period of UV irradiation there was no change. One possible reason for no change is due to saturating the catalyst, leaving a large amount of excess pollutant in the solution; therefore, when aliquot samples were removed for analysis the excess DMMP was masking any degradation that could have been present in solution.

FIG. 34 shows ¹³C NMR-Photocatalysis of DMMP with standard Degussa P25 nanoparticles in DI water over 8 hours of UV irradiation. The experiment was repeated at a lower concentration of 100 μM, the rest of the experimental conditions remained the same except for UV irradiation ended after 4 hours.

FIG. 35 shows ³¹P NMR-Photocatalysis of DMMP with anatase TiO₂nanofibers in water over 4 hours of UV irradiation. Results yielded a decrease in intensity over a 4 hour times period of UV irradiation.

Nanofibrous materials including metal supported nanoparticles on the surface of TiO₂nanofibers can be provided, by including the metal supported nanoparticles in the polyol mixture for electrospinning. SEM/EDX mapping can be used to characterize the final product. FIG. 22 shows SEM/EDX mapping of Pt nanoparticles (purple) supported on the surface of anatase TiO₂nanofibers.

FIGS. 36 and 37 show photocatalysis of 100 μM solution dimethyl methylphosphonate with anatase TiO₂nanofibers in a 100 mL quartz beaker and a 16 ml quartz vial over 2 hours of UV irradiation. FIGS. 36 and 37 show that, after 2 hours of UV irradiation, a reaction vessel with a smaller volume showed a decrease in the signature phosphorus peak. The incident beam of UV irradiation was able to interact with the majority of the sample in the smaller beaker. This allowed for the generation of radicals to increase and react with the pollutant of interest.

Experiments comparing TiO₂nanofibers to nanoparticles as well as Pt nanoparticle doped TiO₂nanofibers were conducted. Pt nanoparticles displaced on the surface of TiO₂should allow for better separation of the electron hole pair under UV and visible irradiation without fear of recombination. Therefore, Pt nanoparticles were dispersed on anatase TiO₂nanofibers via the polyol synthesis:

##STR00002##
Polyol Synthesis of Pt Nanoparticles

These nanofibers were characterized and confirmed using SEM/EDX(mapping) and TEM as seen in FIGS. 9A and 22. FIG. 38 shows TEM imaging of Pt nanoparticles supported on the surface of anatase TiO₂nanofibers.

The Pt—TiO₂catalyst was then introduced to a 100 μM solution of dimethyl methylphosphonate and underwent 4 hours of UV irradiation as seen in FIG. 39. The ³¹P NMR was inconclusive; at 4 hours the signature peak for DMMP seemed to increase in intensity than decrease.

Diameter dependent photocatalysis experiments were also studied. It is hypothesized that the size of the grains that make up the nanofibers plays an important role in photodegradation. Therefore, anatase TiO₂nanofibers were electrospun with 2 different diameter sizes as seen in FIG. 40, which shows SEM (above) & TEM (bottom) images of 2 varying diameters of anatase TiO₂nanofibers ranging from 200 to 300 nm in diameter. These nanofibers were then introduced to a solution of Rhodamine B. in which UV-Vis spectroscopy was used to analyze the photodegradation process. According to Beer's Law, absorbance can be correlated to concentration of Rh.B.

The UV-VIS spectra correlated to the photodegradation of Phenazopyridine (PAP) in FIG. 41A shows the molecular formula of N3. FIGS. 41B and 41C show a UV-VIS spectrogram of N3 solution and UV-VIS of photodegradation of Phenazopyridine (PAP) using N3-sensitized TiO₂nanofiber (from left to right), respectively, showing almost no change when stirred in dark (T=−45 to T=0). Upon UV irradiation the spectra changed near the wavelength of 428 nm which was confirmed to be pure PAP absorption peak. This means N3-dye sensitized TiO₂has the potential to be used as photocatalyst for degradation. FIG. 41D shows that the relative wide band gap of TiO₂limits its application as photocatalyst using under visible light illumination, but that various dyes have narrower band gaps.

After determining the importance of the inner filter effect with the quartz vial and quartz beaker using anatase TiO₂nanofibers, nanofibers and nanoparticles were compared. Degussa P25 nanoparticles were used, which are a standard TiO₂nanoparticle frequently used in literature for photocatalysis experiments. The same experimental conditions were used for each photocatalysis experiment and the results were compared. This can be seen in FIGS. 42 and 43. FIG. 42 shows photocatalysis of 100 μM solution of dimethyl methylphosphonate with Degussa P25 TiO₂nanoparticles over 4 hours of UV irradiation. FIG. 43 shows photocatalysis of 100 μM solution of dimethyl methylphosphonate with anatase TiO₂nanofibers over 2 hours of UV irradiation. After 2 hours of UV irradiation the signature peak for DMMP became undetectable using anatase TiO₂nanofibers where the Degussa P25 nanoparticles require 4 hours of UV irradiation before the signature peak for DMMP became undetectable. These results were confirmed by repetition of the experiment several more times.

The question arose of where the phosphorus was going after the results of the previous experiments were acquired. The phosphorus peak in the NMR was only decreasing in intensity and not shifting or reappearing anywhere else in the spectra. It was then hypothesized that the phosphorus was binding to the TiO₂catalyst and remaining bonded. This was attempted to be confirmed by Raman spectroscopy trying to find a Ti—P stretch of anatase TiO₂nanofibers before and after photocatalysis with DMMP, as shown in FIG. 44. The Raman spectra showed a possible (but unconfirmed) indicator for a PH or PH₂stretch.

Example 5

Polymethylmethacrylate (PMMA) fibers and PMMA/Titanium isopropoxide (TIP) fibers were created through an Electrospinning Procedure performed at 25 kV. The copper wire electrodes were separated by a distance of approximately 4 cm: Solution 1: 640 mg PMMA, 8 mL DMF, 1.32 mL TIP; and Solution 2: 640 mg PMMA, 8 mL DMF (no metal).

Two sol-gel solutions were synthesized. 640 mg PMMA was dissolved in 8 mL DMF for both solutions. However, in only one of the solutions was 1.32 mL Titanium isopropoxide added. Both solutions were added to glass pipettes and sequentially placed on a continuous copper wire which is connected to a high voltage supply source. The solutions were subjected to 25 kV, and once enough charge accumulated the polymer solution was drawn from the pipette to an aluminum foil collector. A dual jet setup for electrospinning polymer fiber blends was employed. FIG. 45 shows an SEM image of blended PMMA/PMMA:TIP polymer fibers. The two large fibers in the center of the image seem to have different surface morphologies and therefore, EDX/mapping was preformed to determine the elemental makeup of these fibers and to confirm distribution of titanium. This can be seen in FIGS. 46, 47 and 48. FIG. 46 shows EDX(mapping) polymer blended nanofibers where blue represents titanium distributed in the matrix. The blue represents the titanium present in the sample. We can tell there is slight Ti density dispersion. However, the density difference is not so significant. It is possible that the fibers might be wet during the spinning and they mix with each other slightly. Therefore, we cannot distinguish the fibers easily. The slight different Ti density dispersion also, might be a hint of our purpose to make a mesh of two types of fibers. FIG. 47 shows EDX(mapping) polymer blended nanofibers where green represents oxygen distributed in the matrix. FIG. 48. EDX(mapping) polymer blended nanofibers where red represents the carbon distributed in the matrix. The SEM images reveal titania dispersion throughout the fibers, making it difficult to discern those fibers with and without the titanium isopropoxide precursor.

Recently, attempts have been made to replicate the photocatalytic degradation of DMMP with TiO₂nanofibers and compare that to the literature standard of Degussa P25 nanoparticles. An experiment was unsuccessful in showing the signature DMMP ³¹P NMR disappear in only 1 hour, as shown in FIG. 49, which shows ³¹P NMR of the photodegradation of 100 μM DMMP with TiO₂nanofibers. However, the P25 nanoparticles showed data consistent with previous results. This implies that the nanofibers were the source of variation in results.

FIGS. 50A and 50B shows that the photocatalytic degradation process is a first-order reaction, and that Anatase/RGO has a higher initial rate constant (k=0.0384 min₋₁) than pure anatase nanoparticles (k=0.0301 min⁻¹) during the first 30 mins degradation.

INVENTORS:

Liu, Jian, Bernier, William E., Jones, Wayne E., Tollin, Julia B., McCarthy, Danielle, Obuya, Emilly, DeCoste, Jared

THIS PATENT IS REFERENCED BY THESE PATENTS:

Patent

Priority

Assignee

Title

THIS PATENT REFERENCES THESE PATENTS:

Patent	Priority	Assignee	Title
7575707,	Mar 29 2005	University of Washington	Electrospinning of fine hollow fibers
7635518,	Feb 04 2005	LOUISIANA AT LAFAYETTE, UNIVERSITY OF	Dendritic magnetic nanostructures and method for making same
7655112,	Jan 31 2002	KX Technologies LLC	Integrated paper comprising fibrillated fibers and active particles immobilized therein
7709088,	Jun 23 2004	Teijin Limited	Inorganic fibers, fiber structure and process for their production
7709597,	May 31 2005	NITTO BOSEKI CO , LTD	Polymer made from organosilane compound and boron compound
7718112,	Aug 23 2004	MASSACHUSETTS, UNIVERSITY OF	Nanometer scale structures
7789930,	Nov 13 2006	Research Triangle Institute	Particle filter system incorporating nanofibers
7931683,	Jul 27 2007	Boston Scientific Scimed, Inc.	Articles having ceramic coated surfaces
7938855,	Nov 02 2007	Boston Scientific Scimed, Inc	Deformable underlayer for stent
7942926,	Jul 11 2007	Boston Scientific Scimed, Inc	Endoprosthesis coating
7976915,	May 23 2007	Boston Scientific Scimed, Inc	Endoprosthesis with select ceramic morphology
7981150,	Nov 09 2006	Boston Scientific Scimed, Inc	Endoprosthesis with coatings
8002823,	Jul 11 2007	Boston Scientific Scimed, Inc	Endoprosthesis coating
8029554,	Nov 02 2007	Boston Scientific Scimed, Inc	Stent with embedded material
8066763,	Apr 11 1998	Boston Scientific Scimed, Inc.	Drug-releasing stent with ceramic-containing layer
8067054,	Apr 05 2007	Boston Scientific Scimed, Inc.	Stents with ceramic drug reservoir layer and methods of making and using the same
8070797,	Mar 01 2007	Boston Scientific Scimed, Inc	Medical device with a porous surface for delivery of a therapeutic agent
8071156,	Mar 04 2009	Boston Scientific Scimed, Inc.	Endoprostheses
8080335,	Jun 09 2006	Canon Kabushiki Kaisha	Powder material, electrode structure using the powder material, and energy storage device having the electrode structure
8187620,	Mar 27 2006	Boston Scientific Scimed, Inc.	Medical devices comprising a porous metal oxide or metal material and a polymer coating for delivering therapeutic agents
8197890,	Feb 04 2005	University of Louisiana at Lafayette	Method of making dendritic magnetic nanostructures
8216632,	Nov 02 2007	Boston Scientific Scimed, Inc	Endoprosthesis coating
8216961,	Aug 27 2008	Korea University Research and Business Foundation	Nanoparticles including metal oxide having catalytic activity
8221822,	Jul 31 2007	Boston Scientific Scimed, Inc	Medical device coating by laser cladding
8225641,	Aug 20 2008	JILIN UNIVERSITY ALAN G MACDIARMID INSTITUTE	Nanofibers and methods of making same and using same in humidity sensors
8231980,	Dec 03 2008	Boston Scientific Scimed, Inc	Medical implants including iridium oxide
8263029,	Aug 25 2008	RESEARCH INSTITUTE FOR CHEMISTRY OF THE HUNGARIAN ACADEMY OF SCIENCES	Method for preparing anisotropic particles and devices thereof
8287937,	Apr 24 2009	Boston Scientific Scimed, Inc.	Endoprosthese
8318126,	May 04 2009		Methods of making metal oxide nanostructures and methods of controlling morphology of same
8329091,	Jan 30 2009	Widener University	Porous metallic structures
8353949,	Sep 14 2006	Boston Scientific Scimed, Inc.	Medical devices with drug-eluting coating
8383539,	Mar 12 2008	Panasonic Corporation	Fiber manufacturing method, fiber manufacturing apparatus and proton-exchange membrane fuel cell
8414806,	Mar 28 2008	Nanyang Technological University; The Board of Trustees of the Leland Stanford Junior University	Membrane made of a nanostructured material
8415267,	Aug 27 2008	Korea University Research and Business Foundation	Nanoparticles including metal oxide having catalytic activity
8431149,	Mar 01 2007	Boston Scientific Scimed, Inc	Coated medical devices for abluminal drug delivery
8449603,	Jun 18 2008	Boston Scientific Scimed, Inc	Endoprosthesis coating
8460547,	Jul 18 2007	Nanyang Technological University; The Board of Trustees of the Leland Stanford Junior University	Hollow porous microspheres
8460790,	Oct 23 2002	TORAY INDUSTRIES, INC	Nanofiber aggregate, polymer alloy fiber, hybrid fiber, fibrous structures, and processes for production of them
8540826,	Oct 02 2009	University of Windsor	Method of surface treatment of aluminum foil and its alloy and method of producing immobilized nanocatalyst of transition metal oxides and their alloys
8562895,	Dec 25 2008	SHINSHU UNIVERSITY; Japan Vilene Company, Ltd.	Process of manufacturing inorganic nanofibers
8574615,	Mar 24 2006	Boston Scientific Scimed, Inc.	Medical devices having nanoporous coatings for controlled therapeutic agent delivery
8585753,	Mar 04 2006		Fibrillated biodegradable prosthesis
8613363,	Jan 31 2002	KX Technologies LLC	Integrated paper comprising fibrillated fibers and active agents immobilized therein
8652229,	Nov 13 2006	Research Triangle Institute	Particle filter system incorporating nanofibers
8684189,	Jul 22 2009	Massachusetts Institute of Technology	Multifunctional electroprocessed membranes
8685424,	Oct 14 2010	ZEUS COMPANY LLC	Antimicrobial substrate
8715855,	Sep 06 2007	Canon Kabushiki Kaisha	Method of producing lithium ion-storing/releasing material, lithium ion-storing/releasing material, and electrode structure and energy storage device using the material
8721923,	Jan 15 2010	The Research Foundation for The State University of New York	Metal sulfide and rare-earth phosphate nanostructures and methods of making same
8771343,	Jun 29 2006	Boston Scientific Scimed, Inc.	Medical devices with selective titanium oxide coatings
8815273,	Jul 27 2007	Boston Scientific Scimed, Inc.	Drug eluting medical devices having porous layers
8815275,	Jun 28 2006	Boston Scientific Scimed, Inc.	Coatings for medical devices comprising a therapeutic agent and a metallic material
8827192,	Sep 21 2007	Lenzing Aktiengesellschaft	Cellulose suspension and processes for its production
8840863,	Sep 04 2008	The Hong Kong University of Science and Technology	Method for synthesising a nano-product
8864341,	Jul 23 2012	Research Triangle Institute	Reflective nanofiber lighting devices
8884507,	Dec 03 2009	Research Triangle Institute	Reflective nanofiber lighting devices
8900292,	Aug 03 2007	Boston Scientific Scimed, Inc	Coating for medical device having increased surface area
8900610,	Aug 30 2004	Southwest Research Institute	Biocidal fibrous and film materials comprising silver and chlorite ions
8906814,	Aug 18 2008	Massachusetts Institute of Technology	Highly reactive multilayer assembled coating of metal oxides on organic and inorganic substrates
8920491,	Apr 22 2008	Boston Scientific Scimed, Inc.	Medical devices having a coating of inorganic material
8921473,	Apr 30 2004		Image making medium
8932346,	Apr 24 2008	Boston Scientific Scimed, Inc.	Medical devices having inorganic particle layers
8940244,	Dec 30 2011	National Tsing Hua University	High thermal stable hollow mesoporous nanotubes, preparation and application for the same
8956910,	Jun 01 2011	Taiwan Textile Research Institute	Method for fabricating photoanode for dye-sensitized solar cell
20080318046,
20140083859,
KR101311604,
KR1020140021947,

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Mar 11 2015	BERNIER, WILLIAM E	The Research Foundation for The State University of New York	ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS	051919	0384	pdf
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Nov 22 2016	OBUYA, EMILY	The Research Foundation for The State University of New York	ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS	051919	0384	pdf

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